Transparent monolithic cubic mesoporous silica synthesized by structure-directing surfactant

The synthesis of transparent monolithic silica with a structure consistent with a space group Pn3m )isdemonstratedusingatemplate-directedsynthesisapproach.TheprocedureisbasedonthehydrolysisandpolymerizationofsiliconalkoxideatlowpHinthepresenceofacationicsurfactant.Thelow-pHreactionrouteischosentoobtaintransparentmonolithicmesoporoussilica.AstructureconsistentwiththePn3m) space group with unit cell lattice parameter ranging from 60–64 Å was identified using small-angle X-ray diffraction. While the lattice parameter is observed to be a monotonically increasing function of surfactant-to-silica ratio, the surfactant-to-alkoxide ratio has a weak discernible effect on the lattice parameter. The Brunauer, Emmett, and Teller (BET) surface area, total pore volume and average pore diameter of the samples are in the range of 787–845 m²/g, 0.37–0.51 cc/g and 18–24 Å respectively. This synthesis approach offers a one-step formation of monolithic mesoporous silica of diverse dimensions for potential use in a variety of technological applications such as catalysis, controlled release and adsorption phenomena . PACS 36.10.Gr; 68.65.-k; 73.21.-b; 73.23.-b     

Synthesis and characterization of ultra-long silica nanowires

Large-scale synthesis of amorphous silica nanowires was achieved by using simple physical evaporation of a mixture of Si and Al₂O₃ powders. Scanning electron microscopy observations showed that the silica nanowires have lengths of several mm and diameters of 20–100 nm. X-ray photoelectron spectroscopy revealed that these nanowires consisted of Si and O elements in an atomic ratio of approximately 1:2, consistent with the stoichiometric formula SiO₂. Photoluminescence measurements showed a blue luminescence band in the wavelength range of 400–500 nm with three peaks at 420 nm, 440 nm, and 470 nm, respectively, which also differs from the previous reports of the photoluminescence for oxygen-deficient silica nanowires. This may suggest that the fully oxidized silica nanowires still have many structural defects that contribute to the photoluminescence. PACS 81.05.Ys; 78.55.Et; 78.30.Fs; 52.75.Rx; 81.15.Gh; 64.70.Fx     

Synthesis and characterization of a hexagonal mesoporous silica with enhanced thermal and hydrothermal stabilities

A synthetic route was developed for a novel hexagonal mesoporous silica that has remarkably wide channel diameters and thick walls. The procedure involved the acid-catalyzed hydrolysis of tetraethylorthosilicate in a water/ethanol/isopropoanol solvent mixture while employing 1-hexadecylamine as a templating agent and mesitylene as an auxiliary agent. After removal of the template by either extraction with ethanolic hydrochloric acid or by calcination at 550 °C, the resulting mesoporous materials had surface areas of 1283 and 1211 m²/g. The channel diameters were found to be 47.2-51.1 Å, while the wall thicknesses were 20.9-21.1 Å. X-ray powder diffraction demonstrated that the novel mesoporous silica belonged to the MCM-41 structural family. Notably, they displayed higher thermal and hydrothermal stabilities, and have higher surface areas than conventionally prepared MCM-41 silica. The thickest channel walls (21.1 Å) can withstand calcination to nearly 850 °C with minimal structural damage. The calcined sample was more resistant to hydrothermal treatment in boiling water than was the solvent-extracted product but both materials showed minimal change after 25 h of hydrothermal treatment.     

Electronic properties of nanocrystalline tin oxide dispersed in monolithic mesoporous silica

This paper is devoted to the study of the electrical properties of nanocrystalline tin oxide dispersed in the mesoporous silica. By immersing the silica in precursor solutions with different concentrations and heat-treatment, different samples were obtained. With precursor concentrations increasing from 0.1 to 4.0 M, the resistivities of the samples decrease from 3.15×10⁶ to 2.43×10³ Ω cm. The resistivity changes with the measurement time, and the deviations from Ohm's law in the voltage–current (V–I) measurements illustrate the capacitance property of these nanocomposites. For this new kind of nanocomposites, the obtained results provide experimental evidence of the conducting mechanism for tin oxide nanoparticles.     

Thickness control of mesoporous silica coated on gold nanorod

Journal of Nanoparticle Research - A Retraction Note to this paper has been published: https://doi.org/10.1007/s11051-021-05224-2     

Synthesis of hematite nanowires using a mesoporous hard template

The influence of the impregnation media (ethanol or water) and the calcination atmosphere (air and NO/He) on the hematite nanowires production embedded on a hard template (MCM-41) was studied. The solids were characterized by X-ray diffraction, Mössbauer spectroscopy and magnetic measurements. The results obtained indicate that the more appropriate conditions for the iron oxide nanowires to get inside the MCM-41 hard template seem to be reached using water as a solvent and air as calcination atmosphere.     

Growth dynamics and thermal stability of Ni nanocrystalline nanowires

The growth dynamics and the thermal stability of a Ni nanocrystalline nanowire (NNW) model system fabricated using electrochemical deposition has been investigated using X-ray diffraction, scanning and transition electron microcopy, and differential scanning calorimetry (DSC). It has been found that the thermal stability of the Ni-NNW is dominated by the microstructure movement and the grain boundary rotation mechanism at temperature ranging from 400 to 600 °C. The Ni-NNW experiences the Rayleigh instability at temperature approaching the melting point. The observed fragment separation in the Rayleigh phase-transition is much greater than that expected theoretically.     

Synthesis of mesoporous silica nanosphere using different templates

Synthesis of mesoporous silica nanosphere were carried out using polyvinyl pyrrolidine and different templates with surfactant property, namely cetyltrimethylammonium bromide, cetyltrimethylammonium chloride, n-octylamine, tetrapropylammonium bromide (TPABr) and these amines give good yield except TPABr. Attempts with other amines without surfactant properties, such as n-propylamine, diethylamine, triethylamine, triethanolamine templates did not give any precipitate in the present reaction scheme. The above synthesis followed by sonication did not change the trend. However addition of dodeycl sodium sulfate surfactant before sonication gave precipitate in all amines, which shows particle growth is induced by surfactant.     

Synthesis of gold nanowires with controlled crystallographic characteristics

The controlled fabrication of poly- and single-crystalline Au nanowires is reported. In polycarbonate templates, prepared by heavy-ion irradiation and subsequent etching, Au nanowires with diameters down to 25 nm are electrochemically synthesized. Four-circle X-ray diffraction and transmission electron microscopy measurements demonstrate that wires deposited potentiostatically at a voltage of -1.2 V at 65 °C are single-crystalline and oriented along the [110] direction. By reverse-pulse electrodeposition, wires oriented along the [100] direction are grown. The wires are cylindrical over their whole length. The morphology of the caps growing on top of poly- and single-crystalline wires is a strong indication of the particular crystalline structure of the nanowires. PACS 61.46.-w; 81.07.-b     

Synthesis and photoluminescence of aligned straight silica nanowires on Si substrate

Aligned straight silica nanowires (NWs) have been synthesized on Si wafer by thermal evaporation of mixed powders of zinc carbonate hydroxide and graphite at 1100 °C and condensation on Si substrate without using any catalyst. The straight silica NWs have diameters ranging from 50 to 100 nm, and lengths of several micrometers, with cone-shaped tips at their ends. High deposition temperature and relatively high SiO_x vapor concentration near the growth substrate would be beneficial to the formation of the aligned straight silica NWs. Different morphologies of silica nanostructures have also been obtained by varying the deposition temperature and the vapor concentration of the SiO_x molecules. Room temperature photoluminescence measurements on the oriented silica NWs show that two green emission bands at 510 and 560 nm, respectively, revealing that the aligned straight silica NWs might have potential applications in the future optoelectronic devices.     

Optical property of nanocomposite of mesoporous silica thin films incorporated with gold nanoparticles

Amino-functionalized mesoporous silica thin films (MTFs) are produced using surface active agent F127,and then gold nanoparticles are introduced into the pore channels to prepare the Au/SiO 2 nanocomposite.After assembling the gold,the amino-functionalized MTF undergoes some shrinkage but remains a periodic structure as demonstrated by X-ray diffraction (XRD) patterns.The nanocomposite shows an acute characteristic diffraction peak assigned to (111) plane of the face-centered-cubic structure of gold,indicating that gold nanoparticles crystallize well and grow in a preferred orientation in the pore channels.The surface plasma resonance (SPR) absorption peak near 570 nm undergoes a red-shift accompanied by a strengthening of intensity when HAuCl 4 is used to react with the amino groups on the internal pore surfaces for 4,6,and 8 h.The simulative results are consistent with the experimental ones shows that the absorption property of the Au/SiO 2 nanocomposite is influenced by the dipping time,which affects the size and volume fraction of embedded gold nanoparticles.     

Temperature and quantum effects in the stability of pure and doped gold nanowires

We investigate, using ab initio molecular dynamics simulations, the effect of temperature on the stability of pure, C and H doped, atomically thin gold nanowires. We show how thermal fluctuations lead to local instabilities that result in the rupture of the nanowires, and how appropriate impurities may help to stabilize these wires. We also show that when light impurity atoms, such as hydrogen, are incorporated in the Au nanowires, quantum effects will affect the nuclear dynamical evolution.     

Adsorption studies of thermal stability of SBA-16 mesoporous silicas

Cage-like ordered mesoporous silicas, SBA-16, and ethane-silicas with cubic (Im3m) and (Fm3m) symmetry groups were synthesized with addition of sodium chloride by using tetraethyl orthosilicate (TEOS) as silica precursor, 1,2-bis(triethoxysilyl)ethane (BTESE) as bridged silsesquioxane and poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide) triblock copolymer Pluronic F127 (EO₁₀₆PO₇₀EO₁₀₆) as template at low acid concentrations. The resulting samples were subjected to extraction in order to remove the polymeric template. The as-synthesized and extracted materials were calcined in the range of 350-900 °C to determine their thermal stability. Based on the XRD analysis and nitrogen adsorption data such as the BET specific surface area, volume of primary mesopores, pore wall thickness and pore size distributions, the SBA-16 silicas exhibit relatively high thermal stability because their mesostructural ordering was retained even up to 900 °C. However, an increase in the calcination temperature tended to decrease significantly the BET surface area, volumes of primary and complementary pores, and to less extent the pore size and pore wall thickness due to the structural shrinkage. Furthermore, the as synthesized samples subjected to a short extraction with acidic ethanol solution possessed even better thermal stability. On the other hand, calcination at 550 °C of ethane-silicas caused a complete removal of the ethane bridging groups from the periodic mesoporous organosilicas and their calcination above 800 °C led to the partial collapse of the structure.     

Structural change of mesoporous silica with sonochemically prepared gold nanoparticles in its pores

Ultrasonic irradiation of mesoporous silica soaked in a mixture of chloroauric acid and isopropanol for 120 min in Ar atmosphere at room temperature yielded Au/SiO₂ mesoporous composite, which was characterized by high resolution transmission electron microscopy and optical absorption measurement. The structure of mesoporous silica after sonochemical preparation of gold (Au) nanoparticles within its pores was studied by nitrogen adsorption technique. It has been shown that the structural parameters, such as specific surface area (SSA), porosity (P), the mean pore diameter (l_p) were increased significantly after ultrasonic irradiation. It is suggested that the collision of Au nanoparticles with pore walls and localized erosion induced by the asymmetric implosive collapse of cavities on the extensive liquid–solid interface that are responsible for the structural change in the mesoporous solid.     

Straight single-crystalline germanium nanowires and their patterns grown on sol-gel prepared gold/silica substrates

Straight single-crystalline Ge nanowires with a uniform diameter distribution of 50-80 nm and lengths up to tens of micrometers were grown in a high yield on sol-gel prepared gold/silica substrates by using Ge powder as the Ge source. Detailed electron microscopy analyses show that the nanowires grow through a vapor-liquid-solid growth mechanism with gold nanoparticles located at the nanowire tips. By using transmission electron microscope grids as the shadow mask, the sol-gel technique can be readily adapted to prepare patterned film-like gold/silica substrates, so that regular micropatterns of Ge nanowires were obtained, which could facilitate the integration of Ge nanowires for characterization and devices.     

Electronic structure effects on stability and quantum conductance in 2D gold nanowires

In this study, we have investigated the stability and conductivity of unsupported, two-dimensional infinite gold nanowires using ab initio density functional theory (DFT). Two-dimensional ribbon-like nanowires with 1–5 rows of gold atoms in the non-periodic direction and with different possible structures have been considered. The nanowires with >2 rows of atoms exhibit dimerization, similar to finite wires, along the non-periodic direction. Our results show that in these zero thickness nanowires, the parallelogram motif is the most stable. A comparison between parallelogram- and rectangular-shaped nanowires of increasing width indicates that zero thickness (111) oriented wires have a higher stability over (100). A detailed analysis of the electronic structure, reveals that the (111) oriented structures show increased delocalization of s and p electrons in addition to a stronger delocalization of the d electrons and hence are the most stable. The density of states show that the nanowires are metallic and conducting except for the double zigzag structure, which is semiconducting. Conductance calculations show transmission for a wide range of energies in all the stable nanowires with more than two rows of atoms. The conductance channels are not purely s and have strong contributions from the d levels, and weak contributions from the p levels.     

碳纳米管内金纳米线的结构与热稳定性

采用分子动力学模拟方法, 研究了填充在(8,8)单壁碳纳米管内的Au纳米线的结构和热稳定性. 研究表明, 经高温退火至室温, Au在碳纳米管内能生成多样而稳定的结构上明显区别于自由状态Au纳米线的壳层螺旋结构Au纳米线, 其螺旋结构会随着温度的变化而转变. 束缚在碳纳米管内的壳层螺旋结构Au纳米线有非常好的热稳定性, 稳定温度高于块体Au晶体的熔化温度. 关键词： 纳米线 碳纳米管 热稳定性 分子动力学模拟     

Preparation and characterization of oriented silica nanowires

Large-scale of oriented closely packed silica nanowire bunches have been synthesized by using large size (1-10 μm in diameter), low melting point tin droplets as catalyst on silicon wafers at 980 °C. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses show that the amorphous silica nanowires have lengths of 50-100 μm and diameters of 100-200 nm. Unlike any previous observed results using high melting point metal (such as gold and iron) as catalyst, the Sn catalyst growth exhibits many interesting phenomena. Each Sn ball can simultaneously catalyze the growth of many silica nanowires, which is quite different from the conventional vapor-liquid-solid process.